Clinical Research Trials Archive – Closed Trials

This is our archive of closed clinical trials, which means that they are no longer accepting new participants or have been concluded. Once a research facility has chosen to close the study, it is sorted into the GPS archive by indication. If you are interested in enrolling in a clinical trial, then please browse our list of active clinical studies.

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We've found
15,419
archived clinical trials in
Pulmonary

Precision of IMED-4 Lung Fluid Measurements
Precision of IMED-4 Lung Fluid Measurements
Status: Enrolling
Updated:  10/13/2015
mi
from
Boston, MA
Precision of IMED-4 Lung Fluid Measurements
Precision of IMED-4 Lung Fluid Measurements
Status: Enrolling
Updated: 10/13/2015
Mass General Hospital
mi
from
Boston, MA
Click here to add this to my saved trials
Precision of IMED-4 Lung Fluid Measurements
Precision of IMED-4 Lung Fluid Measurements
Status: Enrolling
Updated:  10/13/2015
mi
from
Detroit, MI
Precision of IMED-4 Lung Fluid Measurements
Precision of IMED-4 Lung Fluid Measurements
Status: Enrolling
Updated: 10/13/2015
Henry Ford Hospital
mi
from
Detroit, MI
Click here to add this to my saved trials
Precision of IMED-4 Lung Fluid Measurements
Precision of IMED-4 Lung Fluid Measurements
Status: Enrolling
Updated:  10/13/2015
mi
from
Columbus, OH
Precision of IMED-4 Lung Fluid Measurements
Precision of IMED-4 Lung Fluid Measurements
Status: Enrolling
Updated: 10/13/2015
Ohio State University
mi
from
Columbus, OH
Click here to add this to my saved trials
Pulmonary Disease in Patients Undergoing Hematopoietic Stem Cell Transplantation
Pulmonary Disease in Patients Undergoing Hematopoietic Stem Cell Transplantation.
Status: Enrolling
Updated:  10/13/2015
mi
from
Columbus, OH
Pulmonary Disease in Patients Undergoing Hematopoietic Stem Cell Transplantation
Pulmonary Disease in Patients Undergoing Hematopoietic Stem Cell Transplantation.
Status: Enrolling
Updated: 10/13/2015
Ohio State University Medical Center
mi
from
Columbus, OH
Click here to add this to my saved trials
RSV F Dose-Ranging Study in Women
A Phase II Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Multiple Formulations of an RSV F Particle Vaccine With Aluminum, in Healthy Women of Child-Bearing Age
Status: Enrolling
Updated:  10/15/2015
mi
from
Walnut creek, CA
RSV F Dose-Ranging Study in Women
A Phase II Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Multiple Formulations of an RSV F Particle Vaccine With Aluminum, in Healthy Women of Child-Bearing Age
Status: Enrolling
Updated: 10/15/2015
Diablo Clinical Research Inc
mi
from
Walnut creek, CA
Click here to add this to my saved trials
RSV F Dose-Ranging Study in Women
A Phase II Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Multiple Formulations of an RSV F Particle Vaccine With Aluminum, in Healthy Women of Child-Bearing Age
Status: Enrolling
Updated:  10/15/2015
mi
from
Stockbridge, GA
RSV F Dose-Ranging Study in Women
A Phase II Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Multiple Formulations of an RSV F Particle Vaccine With Aluminum, in Healthy Women of Child-Bearing Age
Status: Enrolling
Updated: 10/15/2015
Clincal Research of Atlanta
mi
from
Stockbridge, GA
Click here to add this to my saved trials
RSV F Dose-Ranging Study in Women
A Phase II Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Multiple Formulations of an RSV F Particle Vaccine With Aluminum, in Healthy Women of Child-Bearing Age
Status: Enrolling
Updated:  10/15/2015
mi
from
Boise, ID
RSV F Dose-Ranging Study in Women
A Phase II Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Multiple Formulations of an RSV F Particle Vaccine With Aluminum, in Healthy Women of Child-Bearing Age
Status: Enrolling
Updated: 10/15/2015
Advanced Clinical Research
mi
from
Boise, ID
Click here to add this to my saved trials
RSV F Dose-Ranging Study in Women
A Phase II Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Multiple Formulations of an RSV F Particle Vaccine With Aluminum, in Healthy Women of Child-Bearing Age
Status: Enrolling
Updated:  10/15/2015
mi
from
Lenexa, KA
RSV F Dose-Ranging Study in Women
A Phase II Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Multiple Formulations of an RSV F Particle Vaccine With Aluminum, in Healthy Women of Child-Bearing Age
Status: Enrolling
Updated: 10/15/2015
Johnson County Clin-Trials
mi
from
Lenexa, KA
Click here to add this to my saved trials
RSV F Dose-Ranging Study in Women
A Phase II Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Multiple Formulations of an RSV F Particle Vaccine With Aluminum, in Healthy Women of Child-Bearing Age
Status: Enrolling
Updated:  10/15/2015
mi
from
Springfield, MO
RSV F Dose-Ranging Study in Women
A Phase II Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Multiple Formulations of an RSV F Particle Vaccine With Aluminum, in Healthy Women of Child-Bearing Age
Status: Enrolling
Updated: 10/15/2015
QPS Bio-Kinetic
mi
from
Springfield, MO
Click here to add this to my saved trials
RSV F Dose-Ranging Study in Women
A Phase II Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Multiple Formulations of an RSV F Particle Vaccine With Aluminum, in Healthy Women of Child-Bearing Age
Status: Enrolling
Updated:  10/15/2015
mi
from
Raleigh, NC
RSV F Dose-Ranging Study in Women
A Phase II Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Multiple Formulations of an RSV F Particle Vaccine With Aluminum, in Healthy Women of Child-Bearing Age
Status: Enrolling
Updated: 10/15/2015
Wake Research Associates, LLC
mi
from
Raleigh, NC
Click here to add this to my saved trials
RSV F Dose-Ranging Study in Women
A Phase II Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Multiple Formulations of an RSV F Particle Vaccine With Aluminum, in Healthy Women of Child-Bearing Age
Status: Enrolling
Updated:  10/15/2015
mi
from
Mt. Pleasant, SC
RSV F Dose-Ranging Study in Women
A Phase II Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Multiple Formulations of an RSV F Particle Vaccine With Aluminum, in Healthy Women of Child-Bearing Age
Status: Enrolling
Updated: 10/15/2015
Coastal Carolina Research
mi
from
Mt. Pleasant, SC
Click here to add this to my saved trials
RSV F Dose-Ranging Study in Women
A Phase II Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Multiple Formulations of an RSV F Particle Vaccine With Aluminum, in Healthy Women of Child-Bearing Age
Status: Enrolling
Updated:  10/15/2015
mi
from
Dallas, TX
RSV F Dose-Ranging Study in Women
A Phase II Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Multiple Formulations of an RSV F Particle Vaccine With Aluminum, in Healthy Women of Child-Bearing Age
Status: Enrolling
Updated: 10/15/2015
Research Across America
mi
from
Dallas, TX
Click here to add this to my saved trials
RSV F Dose-Ranging Study in Women
A Phase II Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Multiple Formulations of an RSV F Particle Vaccine With Aluminum, in Healthy Women of Child-Bearing Age
Status: Enrolling
Updated:  10/15/2015
mi
from
San Antonio, TX
RSV F Dose-Ranging Study in Women
A Phase II Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Multiple Formulations of an RSV F Particle Vaccine With Aluminum, in Healthy Women of Child-Bearing Age
Status: Enrolling
Updated: 10/15/2015
Clinical Trials of Texas, Inc.
mi
from
San Antonio, TX
Click here to add this to my saved trials
RSV F Dose-Ranging Study in Women
A Phase II Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Multiple Formulations of an RSV F Particle Vaccine With Aluminum, in Healthy Women of Child-Bearing Age
Status: Enrolling
Updated:  10/15/2015
mi
from
Salt Lake City, UT
RSV F Dose-Ranging Study in Women
A Phase II Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Immunogenicity and Safety of Multiple Formulations of an RSV F Particle Vaccine With Aluminum, in Healthy Women of Child-Bearing Age
Status: Enrolling
Updated: 10/15/2015
Jean Brown Research
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2, Multi-center, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Effects of Inhaled Iloprost on Endurance Time During Cardiopulmonary Exercise Testing in Patients With Pulmonary Hypertension Secondary to Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated:  10/16/2015
mi
from
Torrance, CA
Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2, Multi-center, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Effects of Inhaled Iloprost on Endurance Time During Cardiopulmonary Exercise Testing in Patients With Pulmonary Hypertension Secondary to Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated: 10/16/2015
Los Angeles Biomedical Research Institute
mi
from
Torrance, CA
Click here to add this to my saved trials
Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2, Multi-center, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Effects of Inhaled Iloprost on Endurance Time During Cardiopulmonary Exercise Testing in Patients With Pulmonary Hypertension Secondary to Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated:  10/16/2015
mi
from
Boston, MA
Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2, Multi-center, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Effects of Inhaled Iloprost on Endurance Time During Cardiopulmonary Exercise Testing in Patients With Pulmonary Hypertension Secondary to Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated: 10/16/2015
Massachusetts General Hospital
mi
from
Boston, MA
Click here to add this to my saved trials
Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2, Multi-center, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Effects of Inhaled Iloprost on Endurance Time During Cardiopulmonary Exercise Testing in Patients With Pulmonary Hypertension Secondary to Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated:  10/16/2015
mi
from
Cleveland, OH
Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2, Multi-center, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Effects of Inhaled Iloprost on Endurance Time During Cardiopulmonary Exercise Testing in Patients With Pulmonary Hypertension Secondary to Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated: 10/16/2015
Cleveland Clinic
mi
from
Cleveland, OH
Click here to add this to my saved trials
Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2, Multi-center, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Effects of Inhaled Iloprost on Endurance Time During Cardiopulmonary Exercise Testing in Patients With Pulmonary Hypertension Secondary to Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated:  10/16/2015
mi
from
Oklahoma City, OK
Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2, Multi-center, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Effects of Inhaled Iloprost on Endurance Time During Cardiopulmonary Exercise Testing in Patients With Pulmonary Hypertension Secondary to Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated: 10/16/2015
University of Oklahoma Health Sciences Center
mi
from
Oklahoma City, OK
Click here to add this to my saved trials
Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2, Multi-center, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Effects of Inhaled Iloprost on Endurance Time During Cardiopulmonary Exercise Testing in Patients With Pulmonary Hypertension Secondary to Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated:  10/16/2015
mi
from
Philadelphia, PA
Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2, Multi-center, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Effects of Inhaled Iloprost on Endurance Time During Cardiopulmonary Exercise Testing in Patients With Pulmonary Hypertension Secondary to Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated: 10/16/2015
Temple University Hospital
mi
from
Philadelphia, PA
Click here to add this to my saved trials
Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2, Multi-center, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Effects of Inhaled Iloprost on Endurance Time During Cardiopulmonary Exercise Testing in Patients With Pulmonary Hypertension Secondary to Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated:  10/16/2015
mi
from
Pittsburgh, PA
Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2, Multi-center, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Effects of Inhaled Iloprost on Endurance Time During Cardiopulmonary Exercise Testing in Patients With Pulmonary Hypertension Secondary to Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated: 10/16/2015
University of Pittsburgh Medical Center
mi
from
Pittsburgh, PA
Click here to add this to my saved trials
Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2, Multi-center, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Effects of Inhaled Iloprost on Endurance Time During Cardiopulmonary Exercise Testing in Patients With Pulmonary Hypertension Secondary to Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated:  10/16/2015
mi
from
Jacksonville, FL
Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2, Multi-center, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Effects of Inhaled Iloprost on Endurance Time During Cardiopulmonary Exercise Testing in Patients With Pulmonary Hypertension Secondary to Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated: 10/16/2015
Mayo Clinic, Jacksonville
mi
from
Jacksonville, FL
Click here to add this to my saved trials
Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2, Multi-center, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Effects of Inhaled Iloprost on Endurance Time During Cardiopulmonary Exercise Testing in Patients With Pulmonary Hypertension Secondary to Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated:  10/16/2015
mi
from
Chicago, IL
Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2, Multi-center, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Effects of Inhaled Iloprost on Endurance Time During Cardiopulmonary Exercise Testing in Patients With Pulmonary Hypertension Secondary to Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated: 10/16/2015
Northwestern University
mi
from
Chicago, IL
Click here to add this to my saved trials
Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2, Multi-center, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Effects of Inhaled Iloprost on Endurance Time During Cardiopulmonary Exercise Testing in Patients With Pulmonary Hypertension Secondary to Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated:  10/16/2015
mi
from
New Orleans, LA
Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2, Multi-center, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Effects of Inhaled Iloprost on Endurance Time During Cardiopulmonary Exercise Testing in Patients With Pulmonary Hypertension Secondary to Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated: 10/16/2015
Ochsner Clinic Foundation
mi
from
New Orleans, LA
Click here to add this to my saved trials
Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2, Multi-center, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Effects of Inhaled Iloprost on Endurance Time During Cardiopulmonary Exercise Testing in Patients With Pulmonary Hypertension Secondary to Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated:  10/16/2015
mi
from
Vandoeuvre-lès-Nancy,
Effects of Ventavis in Patients With Pulmonary Hypertension (PH) Secondary to Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2, Multi-center, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Effects of Inhaled Iloprost on Endurance Time During Cardiopulmonary Exercise Testing in Patients With Pulmonary Hypertension Secondary to Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated: 10/16/2015
Hopital d'adultes de Brabois
mi
from
Vandoeuvre-lès-Nancy,
Click here to add this to my saved trials
Outlook Quality of Life Intervention Study
Outlook: An Intervention to Improve Quality of Life in Serious Illness Study
Status: Enrolling
Updated:  10/19/2015
mi
from
Durham, NC
Outlook Quality of Life Intervention Study
Outlook: An Intervention to Improve Quality of Life in Serious Illness Study
Status: Enrolling
Updated: 10/19/2015
Durham VA Medical Center HSR&D COE
mi
from
Durham, NC
Click here to add this to my saved trials
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated:  10/19/2015
mi
from
Birmingham, AL
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated: 10/19/2015
University of Alabama
mi
from
Birmingham, AL
Click here to add this to my saved trials
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated:  10/19/2015
mi
from
Miami, FL
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated: 10/19/2015
Dept of OB/GYN, University of Miami
mi
from
Miami, FL
Click here to add this to my saved trials
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated:  10/19/2015
mi
from
Chicago, IL
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated: 10/19/2015
Northwestern University
mi
from
Chicago, IL
Click here to add this to my saved trials
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated:  10/19/2015
mi
from
Detroit, MI
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated: 10/19/2015
Dept of OB/GYN, Hutzel Hospital
mi
from
Detroit, MI
Click here to add this to my saved trials
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated:  10/19/2015
mi
from
New York, NY
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated: 10/19/2015
St. Luke's Roosevelt Hospital
mi
from
New York, NY
Click here to add this to my saved trials
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated:  10/19/2015
mi
from
Chapel Hill, NC
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated: 10/19/2015
Univ of North Carolina
mi
from
Chapel Hill, NC
Click here to add this to my saved trials
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated:  10/19/2015
mi
from
Winston-Salem, NC
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated: 10/19/2015
Forsyth Memorial Hospital, Wake Forest University School of Medicine
mi
from
Winston-Salem, NC
Click here to add this to my saved trials
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated:  10/19/2015
mi
from
Cincinnati, OH
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated: 10/19/2015
The University Hospital, University of Cincinnati
mi
from
Cincinnati, OH
Click here to add this to my saved trials
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated:  10/19/2015
mi
from
Cleveland, OH
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated: 10/19/2015
Case Western University
mi
from
Cleveland, OH
Click here to add this to my saved trials
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated:  10/19/2015
mi
from
Columbus, OH
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated: 10/19/2015
Dept of OB/GYN, Ohio State University
mi
from
Columbus, OH
Click here to add this to my saved trials
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated:  10/19/2015
mi
from
Philadelphia, PA
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated: 10/19/2015
MCP Hahnemann University
mi
from
Philadelphia, PA
Click here to add this to my saved trials
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated:  10/19/2015
mi
from
Pittsburgh, PA
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated: 10/19/2015
Dept of OB/GYN Magee Womens Hospital
mi
from
Pittsburgh, PA
Click here to add this to my saved trials
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated:  10/19/2015
mi
from
Providence, RI
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated: 10/19/2015
Women and Infants Hospital
mi
from
Providence, RI
Click here to add this to my saved trials
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated:  10/19/2015
mi
from
Dallas, TX
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated: 10/19/2015
Dept of OB/GYN, Southwestern Medical Center, University of Texas
mi
from
Dallas, TX
Click here to add this to my saved trials
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated:  10/19/2015
mi
from
Galveston, TX
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated: 10/19/2015
University of Texas Medical Branch at Galveston
mi
from
Galveston, TX
Click here to add this to my saved trials
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated:  10/19/2015
mi
from
Houston, TX
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated: 10/19/2015
The University of Texas, Houston
mi
from
Houston, TX
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Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated:  10/19/2015
mi
from
Salt Lake City, UT
Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)
Randomized Clinical Trial of the Beneficial Effects of Antenatal Magnesium Sulfate (BEAM)
Status: Enrolling
Updated: 10/19/2015
University of Utah Medical Center
mi
from
Salt Lake City, UT
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SUN11031 in Cachexia Associated With Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2b, Multicenter, Randomized, Double-Blind, Parallel, Placebo-Controlled Study to Evaluate the Efficacy and Safety of SUN11031 for Injection Administered Subcutaneously Twice Daily for 12 Weeks to Subjects Having Cachexia Associated With Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated:  10/19/2015
mi
from
Waterbury, CT
SUN11031 in Cachexia Associated With Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2b, Multicenter, Randomized, Double-Blind, Parallel, Placebo-Controlled Study to Evaluate the Efficacy and Safety of SUN11031 for Injection Administered Subcutaneously Twice Daily for 12 Weeks to Subjects Having Cachexia Associated With Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated: 10/19/2015
Waterbury Pulmonary Associates
mi
from
Waterbury, CT
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SUN11031 in Cachexia Associated With Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2b, Multicenter, Randomized, Double-Blind, Parallel, Placebo-Controlled Study to Evaluate the Efficacy and Safety of SUN11031 for Injection Administered Subcutaneously Twice Daily for 12 Weeks to Subjects Having Cachexia Associated With Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated:  10/19/2015
mi
from
Clearwater, FL
SUN11031 in Cachexia Associated With Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2b, Multicenter, Randomized, Double-Blind, Parallel, Placebo-Controlled Study to Evaluate the Efficacy and Safety of SUN11031 for Injection Administered Subcutaneously Twice Daily for 12 Weeks to Subjects Having Cachexia Associated With Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated: 10/19/2015
Clinical Research of West Florida
mi
from
Clearwater, FL
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SUN11031 in Cachexia Associated With Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2b, Multicenter, Randomized, Double-Blind, Parallel, Placebo-Controlled Study to Evaluate the Efficacy and Safety of SUN11031 for Injection Administered Subcutaneously Twice Daily for 12 Weeks to Subjects Having Cachexia Associated With Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated:  10/19/2015
mi
from
Largo, FL
SUN11031 in Cachexia Associated With Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2b, Multicenter, Randomized, Double-Blind, Parallel, Placebo-Controlled Study to Evaluate the Efficacy and Safety of SUN11031 for Injection Administered Subcutaneously Twice Daily for 12 Weeks to Subjects Having Cachexia Associated With Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated: 10/19/2015
Innovative Research of West Florida
mi
from
Largo, FL
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SUN11031 in Cachexia Associated With Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2b, Multicenter, Randomized, Double-Blind, Parallel, Placebo-Controlled Study to Evaluate the Efficacy and Safety of SUN11031 for Injection Administered Subcutaneously Twice Daily for 12 Weeks to Subjects Having Cachexia Associated With Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated:  10/19/2015
mi
from
Hagerstown, MD
SUN11031 in Cachexia Associated With Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2b, Multicenter, Randomized, Double-Blind, Parallel, Placebo-Controlled Study to Evaluate the Efficacy and Safety of SUN11031 for Injection Administered Subcutaneously Twice Daily for 12 Weeks to Subjects Having Cachexia Associated With Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated: 10/19/2015
The Center for Clinical Research, Washington County Hospital
mi
from
Hagerstown, MD
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SUN11031 in Cachexia Associated With Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2b, Multicenter, Randomized, Double-Blind, Parallel, Placebo-Controlled Study to Evaluate the Efficacy and Safety of SUN11031 for Injection Administered Subcutaneously Twice Daily for 12 Weeks to Subjects Having Cachexia Associated With Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated:  10/19/2015
mi
from
Missoula, MT
SUN11031 in Cachexia Associated With Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2b, Multicenter, Randomized, Double-Blind, Parallel, Placebo-Controlled Study to Evaluate the Efficacy and Safety of SUN11031 for Injection Administered Subcutaneously Twice Daily for 12 Weeks to Subjects Having Cachexia Associated With Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated: 10/19/2015
Montana Medical Research
mi
from
Missoula, MT
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SUN11031 in Cachexia Associated With Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2b, Multicenter, Randomized, Double-Blind, Parallel, Placebo-Controlled Study to Evaluate the Efficacy and Safety of SUN11031 for Injection Administered Subcutaneously Twice Daily for 12 Weeks to Subjects Having Cachexia Associated With Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated:  10/19/2015
mi
from
Papillion, NE
SUN11031 in Cachexia Associated With Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2b, Multicenter, Randomized, Double-Blind, Parallel, Placebo-Controlled Study to Evaluate the Efficacy and Safety of SUN11031 for Injection Administered Subcutaneously Twice Daily for 12 Weeks to Subjects Having Cachexia Associated With Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated: 10/19/2015
The Asthma & Allergy Center, P.C.
mi
from
Papillion, NE
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SUN11031 in Cachexia Associated With Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2b, Multicenter, Randomized, Double-Blind, Parallel, Placebo-Controlled Study to Evaluate the Efficacy and Safety of SUN11031 for Injection Administered Subcutaneously Twice Daily for 12 Weeks to Subjects Having Cachexia Associated With Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated:  10/19/2015
mi
from
Cortland, NY
SUN11031 in Cachexia Associated With Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2b, Multicenter, Randomized, Double-Blind, Parallel, Placebo-Controlled Study to Evaluate the Efficacy and Safety of SUN11031 for Injection Administered Subcutaneously Twice Daily for 12 Weeks to Subjects Having Cachexia Associated With Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated: 10/19/2015
Health Science Research Center - Asthma & Allergy Associates
mi
from
Cortland, NY
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SUN11031 in Cachexia Associated With Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2b, Multicenter, Randomized, Double-Blind, Parallel, Placebo-Controlled Study to Evaluate the Efficacy and Safety of SUN11031 for Injection Administered Subcutaneously Twice Daily for 12 Weeks to Subjects Having Cachexia Associated With Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated:  10/19/2015
mi
from
Cincinnati, OH
SUN11031 in Cachexia Associated With Chronic Obstructive Pulmonary Disease (COPD)
A Phase 2b, Multicenter, Randomized, Double-Blind, Parallel, Placebo-Controlled Study to Evaluate the Efficacy and Safety of SUN11031 for Injection Administered Subcutaneously Twice Daily for 12 Weeks to Subjects Having Cachexia Associated With Chronic Obstructive Pulmonary Disease
Status: Enrolling
Updated: 10/19/2015
New Horizons Clinical Research
mi
from
Cincinnati, OH
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